| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377624-149377863 | Common:1; Rare:55 | ||||
| chr3:149813117-149813291 | Common:1; Rare:62 | ||||
| chr3:149971151-149971354 | Common:3; Rare:97 | ||||
| chr3:150408170-150408308 | Common:1; Rare:54 | ||||
| chr3:150603145-150603342 | Common:2; Rare:71 | ||||
| chr3:151340819-151340899 | Rare:17 | ||||
| chr3:152268838-152268978 | Rare:55 | ||||
| chr3:152269544-152269691 | Rare:39 | ||||
| chr3:154121308-154121444 | Common:2; Rare:62 | ||||
| chr3:154324402-154324571 | Rare:68 | ||||
| chr3:155854350-155854774 | Rare:117 | ||||
| chr3:156555059-156555419 | Common:2; Rare:135 | ||||
| chr3:156674339-156674618 | Common:4; Rare:80 | ||||
| chr3:157160065-157160288 | Rare:94 |